Search details
1.
Vici syndrome in siblings born to consanguineous parents.
Am J Med Genet A
; 170A(1): 220-5, 2016 Jan.
Article
in English
| MEDLINE | ID: mdl-26395118
2.
Carbonic Anhydrase VI Gene Polymorphism rs2274327 Relationship Between Salivary Parameters and Dental-Oral Health Status in Children.
Biochem Genet
; 54(4): 467-475, 2016 Aug.
Article
in English
| MEDLINE | ID: mdl-27100223
3.
Mitochondrial DNA deletions in patients with chronic suppurative otitis media.
Eur Arch Otorhinolaryngol
; 273(9): 2473-9, 2016 Sep.
Article
in English
| MEDLINE | ID: mdl-26620342
4.
A novel insertion mutation identified in exon 10 of the MEFV gene associated with Familial Mediterranean Fever.
BMC Med Genet
; 15: 74, 2014 Jul 01.
Article
in English
| MEDLINE | ID: mdl-24980720
5.
A rare cause of dyspnea in emergency medicine: Keutel syndrome.
Am J Emerg Med
; 34(5): 935.e3-5, 2016 May.
Article
in English
| MEDLINE | ID: mdl-26462901
6.
Unbalanced 3;22 translocation with 22q11 and 3p deletion syndrome.
Am J Med Genet A
; 152A(11): 2791-5, 2010 Nov.
Article
in English
| MEDLINE | ID: mdl-20949503
7.
Increased EGFR mRNA Expression Levels in Non-Small Cell Lung Cancer.
Eurasian J Med
; 51(2): 177-185, 2019 Jun.
Article
in English
| MEDLINE | ID: mdl-31258360
8.
Anticancer, Antioxidant and Cytotoxic Potential of Thymol in vitro Brain Tumor Cell Model.
Cent Nerv Syst Agents Med Chem
; 17(2): 116-122, 2017.
Article
in English
| MEDLINE | ID: mdl-27554922
9.
Correlation with Platelet Parameters and Genetic Markers of Thrombophilia Panel (Factor II g.20210G>A, Factor V Leiden, MTHFR (C677T, A1298C), PAI-1, ß-Fibrinogen, Factor XIIIA (V34L), Glycoprotein IIIa (L33P)) in Ischemic Strokes.
Neuromolecular Med
; 18(2): 170-6, 2016 Jun.
Article
in English
| MEDLINE | ID: mdl-26951304
10.
Association Between Human Hair Loss and the Expression Levels of Nucleolin, Nucleophosmin, and UBTF Genes.
Genet Test Mol Biomarkers
; 20(4): 197-202, 2016 Apr.
Article
in English
| MEDLINE | ID: mdl-26866305
11.
The Relationship Between Endothelial Nitric Oxide Synthase Gene (NOS3) Polymorphisms, NOS3 Expression, and Varicocele.
Genet Test Mol Biomarkers
; 20(4): 191-6, 2016 Apr.
Article
in English
| MEDLINE | ID: mdl-26866567
12.
Differential expressions of cancer-associated genes and their regulatory miRNAs in colorectal carcinoma.
Gene
; 567(1): 81-6, 2015 Aug 01.
Article
in English
| MEDLINE | ID: mdl-25925209
13.
Does the level of WT1 expression predict the outcome in Philadelphia-negative myeloproliferative neoplasms?
Genet Test Mol Biomarkers
; 19(4): 222-4, 2015 Apr.
Article
in English
| MEDLINE | ID: mdl-25714774
14.
Association of endothelial nitric oxide synthase gene polymorphisms (894G/T, -786T/C, G10T) and clinical findings in patients with migraine.
Neuromolecular Med
; 16(3): 587-93, 2014 Sep.
Article
in English
| MEDLINE | ID: mdl-24845269
15.
Combined occurrence of Alström syndrome and bronchiectasis.
Pediatrics
; 133(3): e780-3, 2014 Mar.
Article
in English
| MEDLINE | ID: mdl-24534407
16.
Holoprosencephaly: ZIC2 mutation in a case with panhypopituitarism.
J Pediatr Endocrinol Metab
; 27(7-8): 777-81, 2014 Jul.
Article
in English
| MEDLINE | ID: mdl-24706429
17.
Anticancer and antioxidant properties of terpinolene in rat brain cells.
Arh Hig Rada Toksikol
; 64(3): 415-24, 2013 Sep.
Article
in English
| MEDLINE | ID: mdl-24084350
18.
Frank-ter Haar syndrome with unusual clinical features.
Eur J Med Genet
; 52(4): 247-9, 2009.
Article
in English
| MEDLINE | ID: mdl-19303467
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